A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730426



Internal ID20506338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126484465..126484974hg38UCSC Ensembl
chr9:129246744..129247253hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292215
Samples
Known GenesMVB12B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730426
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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